Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2569190
CD14 ; TMCO6
0.620 0.560 5 140633331 intron variant A/G snv 0.57 39
rs4950928
CHI3L1
0.653 0.560 1 203186754 upstream gene variant G/A;C;T snv 33
rs1861494
IFNG-AS1 ; IFNG
0.716 0.400 12 68157629 intron variant C/T snv 0.75 15
rs1207011218
CTLA4
0.742 0.440 2 203870794 synonymous variant C/T snv 12
rs2872507 0.752 0.360 17 39884510 intergenic variant G/A;T snv 12
rs324011
STAT6
0.742 0.360 12 57108399 intron variant C/T snv 0.32 12
rs7927894 0.742 0.320 11 76590272 upstream gene variant C/T snv 0.35 12
rs4794820
LRRC3C
0.790 0.160 17 39933091 intron variant A/G;T snv 9
rs12603332
LOC112268187 ; ORMDL3 ; LRRC3C
0.807 0.200 17 39926554 5 prime UTR variant T/C snv 0.49 7
rs4794067
TBX21
0.807 0.280 17 47731462 upstream gene variant T/A;C snv 0.25 7
rs928413
IL33
0.807 0.120 9 6213387 upstream gene variant G/A;C snv 7
rs2664538
MMP9
0.827 0.200 20 46011586 missense variant A/G snv 6
rs4065275
ORMDL3
0.807 0.160 17 39924612 intron variant A/G;T snv 0.56 6
rs324015
STAT6
0.827 0.120 12 57096317 3 prime UTR variant T/C snv 0.76 5
rs6871536
RAD50 ; TH2LCRR
0.827 0.160 5 132634182 intron variant T/C snv 0.24 5
rs10494132
CHIA
0.851 0.080 1 111289601 upstream gene variant T/C snv 0.26 4
rs1999071 0.851 0.080 14 22659998 regulatory region variant T/C snv 0.29 4
rs1558641
IL1R1
0.925 0.080 2 102149405 intron variant G/A snv 0.13 3
rs2233407
NFKBIA
0.882 0.080 14 35405317 upstream gene variant T/A;C snv 3
rs4559
NAB2 ; STAT6
0.882 0.080 12 57095865 3 prime UTR variant C/T snv 0.59 3
rs71802646
STAT6
0.882 0.080 12 57111290 5 prime UTR variant ACACACACACACACAC/-;AC;ACAC;ACACAC;ACACACAC;ACACACACAC;ACACACACACAC;ACACACACACACAC;ACACACACACACACACAC;ACACACACACACACACACAC;ACACACACACACACACACACAC;ACACACACACACACACACACACAC;ACACACACACACACACACACACACAC delins 0.32 3
rs73985228
ORMDL3
0.882 0.080 17 39922412 3 prime UTR variant G/C;T snv 3
rs16947078 0.925 0.080 17 47748134 downstream gene variant A/G;T snv 2
rs2236648
STIP1
0.925 0.080 11 64197185 intron variant C/T snv 0.39 2
rs2282290
CHIA
0.925 0.080 1 111320829 intron variant A/G snv 0.38 2